Evidence map›Paper›PMID 26424808›Full record

ArticlePathogens and disease2015

Potential role of autophagy in the bactericidal activity of human PMNs for Bacillus anthracis.

Girish Ramachandran, Padmaja Gade, Pei Tsai, Wuyuan Lu, Dhananjaya V Kalvakolanu, Gerald M Rosen, Alan S Cross

Open access · bronzeAbstract read
In one paragraph

Article in Pathogens and disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Autophagy in neutrophils.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2020
    Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Innate Immune Interactions betweenFrontiers in cellular and infection microbiology · 2018
    Article
  8. Article
  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Girish RamachandranCenter for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD 21201, USA gramacha@medicine.umaryland.edu.
Padmaja GadeDepartment of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Pei TsaiDepartment of Pharmaceutical Sciences, and the Center for EPR Imaging In Vivo Physiology, University of Maryland School of Pharmacy, Baltimore, MD 21201, USA.
Wuyuan LuInstitute of Human Virology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Dhananjaya V KalvakolanuDepartment of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Gerald M RosenDepartment of Pharmaceutical Sciences, and the Center for EPR Imaging In Vivo Physiology, University of Maryland School of Pharmacy, Baltimore, MD 21201, USA.
Alan S CrossCenter for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
University of Maryland, Baltimore · US

Funding

PHS HHS NIH U54 A1057 168-05
6 · The paper itself

Abstract

Bacillus anthracis, the causative agent of anthrax, is acquired by mammalian hosts from the environment, as quiescent endospores. These endospores must germinate inside host cells, forming vegetative bacilli, before they can express the virulence factors that enable them to evade host defenses and disseminate throughout the body. While the role of macrophages and dendritic cells in this initial interaction has been established, the role of polymorphonuclear leukocytes (PMNs) has not been adequately defined. We discovered that while B. anthracis 34F2 Sterne endospores germinate poorly within non-activated human PMNs, these phagocytes exhibit rapid microbicidal activity toward the outgrown vegetative bacilli, independent of superoxide and nitric oxide. These findings suggest that a non-free radical pathway kills B. anthracis bacilli. We also find in PMNs an autophagic mechanism of bacterial killing based on the rapid induction of LC-3 conversion, beclin-1 expression, sequestosome 1 (SQSTM1) degradation and inhibition of bactericidal activity by the inhibitor, 3-methyladenine. These findings extend to PMNs an autophagic bactericidal mechanism previously described for other phagocytes.

Indexed as

AutophagyMicrobial ViabilityAnimalsAnthraxBacillus anthracisBlotting, WesternCells, CulturedHumansMiceNeutrophilsPhagocytosisReactive Nitrogen SpeciesReactive Oxygen SpeciesReactive Nitrogen SpeciesReactive Oxygen SpeciesautophagyB. anthracisneutrophilsphagocytosis

Identifiers

PMID26424808
PMCPMC4626618
OpenAlexW2172420694

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.